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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc2a5
solute carrier family 2 (facilitated glucose transporter), member 5
MGI:1928369
11 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc2a5tm1.1Jnz/Slc2a5tm1.1Jnz
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
normal hearing/vestibular/ear phenotype J:136820
Slc2a5tm1b(EUCOMM)Wtsi/Slc2a5tm1b(EUCOMM)Wtsi
C57BL/6N-Slc2a5tm1b(EUCOMM)Wtsi/Ieg
abnormal lens morphology J:211773
abnormal ovary morphology J:211773
abnormal retina morphology J:211773
abnormal seminal vesicle morphology J:211773
cataract J:211773
decreased exploration in new environment J:211773
enlarged lymph nodes J:211773
enlarged spleen J:211773
hydrometra J:211773
persistence of hyaloid vascular system J:211773

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory